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Biosample Operations Manager Pharmaceutical

Location: Cambridge, MA
Job Type: Contract
Salary: $1.00 - $1.00
Hourly: $1.00 - $1.00
Date: 4/16/2018
Job ID: 02589752
Job Description
Global Pharmaceutical company which focuses in Rare Disease, Oncology and Infectious Disease is hiring a
Biosmaple Operations Manager
Must have GCP  experience and Sponsor experience (Biotech or Pharmaceutical)
One year w-2 contract with full benefits offered
Or can go permanent Full time
Send resume if interested and qualified:Company is seeking a Biosample Operations Manager to support the clinical teams and  to work across its projects as well as with the external biorepositories, assay laboratories and CROs.  This position may report directly to the Company’s Head of Therapeutic Operations or to a Clinical Biomarker Director.  This position will work collaboratively across all therapeutic area teams for to ensure implementation, compliance and support of biosample management for clinical trials conducted by Company.
Responsibilities
  • In collaboration with individuals from Clinical Biomarker Director and Research groups to support the evaluation of technologies to identify, define and implement the biomarker strategy to support the clinical development of Company’s compounds
  • Provide support  to the clinical teams driving agreed upon biomarker sample management for the clinical projects.
  • Support the review of the biomarker sections of the clinical protocol, study/lab manuals and consent forms
  • Build cross functional process for sample flow, biorepository usage
  • Develop and provide ongoing sample training to team members 
  • May participate in committees and work streams that support process and procedure for standardized language, biomarker usage, and data reporting
  • Work with clinical sites, as needed, to ensure accurate and appropriate sample collection to support the biomarker strategy
  • Serve as a point of contact for the biomarker sample repository
  • Support the Clinical Biomarker Directors in the analyses of biomarker data, collaborating with biostatisticians, bioinformatics, clinical and research team members
  • Support teams to ensure biosamples are compliant with informed consent and GCP/ICH
Qualifications
  • Bachelor’s degree in a science-based subject; Advanced degree preferred
  • Minimum of 5 years of clinical research experience which must include sponsor experience
  • Direct experience with clinical sample management
  • Prior process development experience needed
  • Familiarity with databases is essential
  • Solid understanding of good Clinical GCP/ICH is required.
  • Strong communication skills and attention to detail
 

 

 

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